Clinical Study Manager Jobs in Minnesota (NOW HIRING)

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Title: Sr. Clinical Research Specialist
Location: Minneapolis, MN
Duration: 24+Months (Possibility of extension)
Local candidate to Minneapolis, MN needed
Position Description:

The Sr. Clinical Research Specialist (Sr. CRS) will support the execution of clinical research activities related to the ongoing evaluation of product safety and effectiveness following market release.

Under supervision, the Sr. CRS may assume project management responsibilities for assigned studies and will be responsible for the timely completion of deliverables consistent with applicable regulatory standards and internal Healthcare requirements.
Position Responsibilities:

Prepare and revise study materials and/or training

Conduct training of site and/or Healthcare staff

Assist in site initiation activities (e.g. study start-up documentation preparation)

Set-up and maintain accurate progress and study status tracking logs

Assist in the preparation of reports, regulatory submissions, publications and presentations

Assist in the preparation of budgets and project plans

Identify and mitigate quality risk and/or issues associated with assigned studies/activities

May arrange conference calls, staff meetings, and training events.

Assist in the preparation and review of data

Oversee follow-up and resolution of sites issues

Oversee activities performed by extended team members including work direction (e.g. project coordinators, monitors, safety and data specialists, etc.) to ensure compliance with protocol, appropriate regulations and guidelines

Able to refer to Standard Operating Procedures (SOPs) and study management processes for guidance on everyday tasks

Contribute to process improvement initiatives and participate in training to enhance knowledge

Basic Qualifications:

Bachelor's degree

4+ years' experience in clinical research (Master's degree will substitute for 1 year experience)

Desired/Preferred Qualifications:
Working knowledge of Good Clinical Practice (GCP) and regulatory compliance guidelines for conducting clinical studies
Proficient knowledge of medical terminology
Computer skill competency (MS Office products, spreadsheets, power points, etc.)
Ability to work well within teams, build relationships
Good prioritization and organizational skills, able to manage multiple tasks
Excellent oral and written communication
Positive outlook
Strong communication skills (efficient, effective, transparent)
Physical Job Requirements:

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to be independently mobile.

The employee is also required to interact with a computer, and communicate with peers and co-workers.

Ability to travel 10-20%

We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

Thanks & Regards,

Seema Chawhan

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

DIRECT # - 732-844-8724

Email id - seema @irionline.com| www.irionline.com 

LinkedIn: https://in.linkedin.com/in/seemachawhan

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